Clinical Supply Chain Specialist
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands.
- Create and maintain study forecast for finished drug product in applicable systems to support clinical study start
- Design optimal packaging configuration for finished drug product taking into account protocol requirements and product characteristics.
- Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within our supply chain network (both internal and external) to support global study footprint.
- Design cost efficient (re)supply model to distribute finished drug product by taken into account risk analysis and mitigation strategy.
- Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenario’s, impact on study demand and set up activities for formulation and device introductions
- Bachelor degree or equivalent in logistics, business administration or life science.
- Typically 5 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
- At minimum 3 year experience in project leadership and project management
techniques in an international and regulated environment
- General understanding of regulatory guidelines impacting clinical supplies
(i.e. GxP, ICH guidelines, Clinical Trial Directive)
- Fluency in English, both verbal and written communication
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
The Company
They are an international company with locations all over the world. This job position is located in Breda.Role Description
You will develop and employ project management techniques to design and set up supply chains for clinical studies.Responsibilities
- Create and maintain project plan to ensure timely clinical study start to support first subject enrolled per country cluster/ depot- Create and maintain study forecast for finished drug product in applicable systems to support clinical study start
- Design optimal packaging configuration for finished drug product taking into account protocol requirements and product characteristics.
- Ensure storage and shipping capabilities plus sufficient capacity for finished drug product is available within our supply chain network (both internal and external) to support global study footprint.
- Design cost efficient (re)supply model to distribute finished drug product by taken into account risk analysis and mitigation strategy.
- Facilitate the phase in phase out strategy for new medicinal product introduction, such as running scenario’s, impact on study demand and set up activities for formulation and device introductions
Requirements
- Knowledge of clinical supply chain management- Bachelor degree or equivalent in logistics, business administration or life science.
- Typically 5 year’s relevant working experience, preferably in the biotechnology or pharmaceutical industry, with an in-depth knowledge of supply chain management and clinical research management principles.
- At minimum 3 year experience in project leadership and project management
techniques in an international and regulated environment
- General understanding of regulatory guidelines impacting clinical supplies
(i.e. GxP, ICH guidelines, Clinical Trial Directive)
- Fluency in English, both verbal and written communication
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
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